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Inhibitory effect of interferon-α-2b on expression of cyclooxygenase-2 and vascular endothelial growth factor in human hepatocellular carcinoma inoculated in nude mice

机译:干扰素-α-2b对裸鼠接种人肝细胞癌中环氧合酶-2和血管内皮生长因子表达的抑制作用

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AIM: To evaluate the effects of interferon-α-2b (IFN-α-2b) on expression of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF) in human hepatocellular carcinoma (HCC) inoculated in nude mice and to study the underlying mechanism of IFN-α-2b against HCC growth.METHODS: Thirty-two nude mice bearing human HCC were randomly divided into four groups (n = 8). On the 10th day after implantation of HCC cells, the mice in test groups (groups A, B and C) received IFN-α-2b at a serial dose (10 000 IU for group A, 20 000 IU for group B, 40 000 IU for group C sc daily) for 35 d. The mice in control group received normal saline (NS). The growth conditions of transplanted tumors were observed. Both genes and proteins of COX-2 and VEGF were detected by RT-PCR and Western blot. Apoptosis of tumor cells in nude mice was detected by TUNEL assay after treatment with IFN-α-2b.RESULTS: Tumors were significantly smaller and had a lower weight in the IFN-α-2b treatment groups than those in the control group (P < 0.01), and the tumor growth inhibition rate in groups A, B and C was 27.78%, 65.22% and 49.64%, respectively. The expression levels of both genes and proteins of COX-2 and VEGF were much lower in the IFN-α-2b treatment groups than in the control group (P < 0.01). The apoptosis index (AI) of tumor cells in the IFN-α-2b treatment groups was markedly higher than that in the control group (P < 0.01). Group B had a higher inhibition rate of tumor growth, a lower expression level of COX-2 and VEGF and a higher AI than groups A and C (P < 0.05), but there was no significant difference between groups A and C.CONCLUSION: The inhibitory effects of IFN-α-2b on implanted tumor growth and apoptosis may be associated with the down-regulation of COX-2 and VEGF expression. There is a dose-effect relationship. The medium dose of IFN-α-2b for inhibiting tumor growth is 20 000 IU/d.
机译:目的:评价干扰素-α-2b(IFN-α-2b)对裸鼠和人肝细胞癌中环氧合酶2(COX-2)和血管内皮生长因子(VEGF)表达的影响。方法:将32只带有人肝癌的裸鼠随机分为四组(n = 8)。在植入HCC细胞后的第10天,测试组(A,B和C组)的小鼠接受了连续剂量的IFN-α-2b(A组为10 000 IU,B组为20 000 IU,B组为40 000 C组每天IU(IU)35天。对照组的小鼠接受生理盐水(NS)。观察移植肿瘤的生长状况。 RT-PCR和Western blot检测COX-2和VEGF的基因和蛋白。 IFN-α-2b治疗后,通过TUNEL法检测裸鼠的肿瘤细胞凋亡。结果:IFN-α-2b治疗组的肿瘤明显小于对照组,且重量较对照组低(P < 0.01),A,B和C组的肿瘤生长抑制率分别为27.78%,65.22%和49.64%。 IFN-α-2b治疗组的COX-2和VEGF基因和蛋白的表达水平均低于对照组(P <0.01)。 IFN-α-2b治疗组的肿瘤细胞凋亡指数(AI)明显高于对照组(P <0.01)。与A,C组相比,B组对肿瘤生长的抑制率更高,COX-2和VEGF的表达水平较低,AI较高(P <0.05),但A,C组之间无显着差异。 IFN-α-2b对植入的肿瘤生长和凋亡的抑制作用可能与COX-2和VEGF表达的下调有关。存在剂量效应关系。抑制肿瘤生长的IFN-α-2b中等剂量为20 000 IU / d。

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